Combined disinfection and decontamination agent having increased effectiveness
The invention relates to a novel combined disinfection and decontamination agent comprising at least one vitamin, at least one metal ion, at least one active-surface compound, and at least one further antimicrobial active substance. The agent according to the invention surprisingly shows nearly complete nucleic acid disintegration in addition to an improved disinfectant effect. The agent can be successfully used as a combined decontamination and disinfection agent for skin, mucous membranes, hands, wounds, and/or hair, and instruments and surfaces of all kinds.
1. A method for the decontamination and disinfection of animate surfaces, comprising applying an effective amount of the composition (i) vitamin C, (ii) between .01-100 mM of a metal ion FeCl 3 , or CuCl 2 , (iii) at least one surface-active compound and (iv) at least one antimicrobial active substance, selected from the group consisting of ethanol, 1-propanol, 2-propanol, lactic acid, benzalkonium chloride, didecyldimethyl ammonium chloride, glutaric dialdehyde 1,2-pentane diol, or a mixture thereof.
2. The method according to claim 1 , wherein the animated surface is selected from the group consisting of skin, hairs mucous membranes, wounds, or hands.
3. A method for the decontamination and disinfection of inanimate surfaces, comprising applying an effective amount of the composition (i) vitamin C, (ii) between .01-100 mM of a metal ion FeCl 3 , or CuCl 2 , (iii) at least one surface-active compound and (iv) at least one antimicrobial active substance, selected from the group consisting of ethanol, 1-propanol, 2-propanol, lactic acid, benzalkonium chloride, didecyldimethyl ammonium chloride, glutaric dialdehyde, 1,2-pentane diol, or a mixture thereof.
4. The method according to claim 3 , wherein the inanimate surface is a part of an instrument or surfaces.
5. A method for the production of an agent for the degradation of biofilm an effective amount of the composition comprising (i)vitamin C, (ii) between .01-100 mM of a metal ion FeCl 3 , or CuCl 2 , (iii) at least one surface-active compound and (iv) at least one antimicrobial active substance, selected from the group consisting of ethanol, 1-propanol, 2-propanol, lactic acid, benzalkonium chloride, didecyldimethyl ammonium chloride, glutaric dialdehyde, 1,2-pentane diol, or a mixture thereof.
6. The method according to claim 1 , wherein the at least one surface-active compound is selected from the group consisting of anionic, non-ionic, amphoteric or cationic surfactants, and a mixture thereof.
7. The method according to claim 3 , wherein the at least one surface-active compound is selected from the group consisting of anionic, non-ionic, amphoteric or cationic surfactants, and a mixture thereof.
8. The method according to claim 5 , wherein the composition additionally contains an antimicrobial active substance which is an alcoholic active substance selected from the group consisting of methanol, ethanol, 1-propanol, 2-propanol, butanol, chlorobutanol, pentanol or hexanol, propylene glycol, polyethylene glycol, triethylene glycol, hexyldiglycol, butylene glycol, pentanediol, hexanediol, heptanediol, octanediol, decanediol, glycerol, 1,2- or 1,3 diols or hexyldiglycol, 2-bromo-2-nitropropane diol, 5-bromo-5-nitro-1,3 dioxane, benzyl alcohol, chlorobenzyl alcohol, phenylethyl alcohol, phenoxy ethanol, 1,2-phenoxypropanol, 1,3-phenoxypropanol or mixtures thereof.
9. The method according to claim 5 , wherein the composition additionally contains an antimicrobial active substance which is a formaldehyde eliminator and/or eliminator of dialdehydes.
10. The method according to claim 5 , wherein the at least one surface-active compound is selected from the group consisting of anionic, non-ionic, amphoteric or cationic surfactants, and a mixture thereof.
11. The method according to claim 1 , wherein metal ion is present in a concentration of between .01-50 mM.
12. The method according to claim 1 , wherein the metal ion is present in a concentration of between .01-10 mM.
13. The method according to claim 3 , wherein the metal ion is present in a concentration of between .01-50 mM.
14. The method according to claim 3 , wherein the metal ion is present in a concentration of between .01-10 mM.
15. The method according to claim 5 , wherein the metal ion is present in a concentration of between .01-50 mM.
16. The method according to claim 5 , wherein the metal ion is present in a concentration of between .01-10 mM.